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Author Details

P??ivi Onkamo
University of Turku
1999
47
21
PMIDPaper TitleJournal TitlePublished Year
36513080Genetic admixture and language shift in the medieval Volga-Oka interfluve.Curr Biol2023
35393601Emergence and intensification of dairying in the Caucasus and Eurasian steppes.Nat Ecol Evol2022
34618559Ten millennia of hepatitis B virus evolution.Science2021
32315354Buried in water, burdened by nature-Resilience carried the Iron Age people through Fimbulvinter.PLoS One2020
32795443Ancient Bacterial Genomes Reveal a High Diversity of Treponema pallidum Strains in Early Modern Europe.Curr Biol2020
31729399Human mitochondrial DNA lineages in Iron-Age Fennoscandia suggest incipient admixture and eastern introduction of farming-related maternal ancestry.Sci Rep2019
30479341Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe.Nat Commun2018
28733587Identification and analysis of mtDNA genomes attributed to Finns reveal long-stagnant demographic trends obscured in the total diversity.Sci Rep2017
28611769Analysis of Complement <i>C3</i> Gene Reveals Susceptibility to Severe Preeclampsia.Front Immunol2017
26909693Creative Activities in Music--A Genome-Wide Linkage Analysis.PLoS One2016
28004803Convergent evidence for the molecular basis of musical traits.Sci Rep2016
24614497A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.Mol Psychiatry2015
26132657Vestiges of an Ancient Border in the Contemporary Genetic Diversity of North-Eastern Europe.PLoS One2015
26154559The genetic variant rs4073 Aâ¿¿T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration.Acta Ophthalmol2015
25707602Association and Promoter Analysis of AVPR1A in Finnish Autism Families.Autism Res2015
22998103Correlation between components of newly diagnosed exudative age-related macular degeneration lesion and focal retinal sensitivity.Acta Ophthalmol2014
25080345Neolithic dairy farming at the extreme of agriculture in northern Europe.Proc Biol Sci2014
23584701Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration.Retina2013
22018929Genetic background and the risk of otitis media.Int J Pediatr Otorhinolaryngol2012
22380611Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria.Malar J2012
21203819SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.Behav Genet2011
21307861Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music.J Hum Genet2011
20410850Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample.Psychiatr Genet2010
20122735Screening of DNA-variants in the properdin gene (CFP) in age-related macular degeneration (AMD).Mol Immunol2010
19461995Musical aptitude is associated with AVPR1A-haplotypes.PLoS One2009
19999660[Identification of susceptibility genes for age-related macular degeneration--a success story of molecular genetics].Duodecim2009
19997561Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE).PLoS One2009
19343041Association of LOXL1 gene with Finnish exfoliation syndrome patients.J Hum Genet2009
18413417Clinical and laboratory characteristics of Finnish lupus erythematosus patients with cutaneous manifestations.Lupus2008
19048105Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration.PLoS One2008
17340018Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis.Acta Derm Venereol2007
17309879A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.Hum Mol Genet2007
16288313Genome scan on Swedish Alzheimer's disease families.Mol Psychiatry2006
16595078A survey of data mining methods for linkage disequilibrium mapping.Hum Genomics2006
16258007An empirical comparison of case-control and trio based study designs in high throughput association mapping.J Med Genet2006
15054392Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus.Eur J Hum Genet2004
15007729Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.Hum Genet2004
15059244Increasing incidence of Type 1 diabetes--role for genes?BMC Genet2004
12097292A novel low-penetrance locus for familial glioma at 15q23-q26.3.Cancer Res2002
12485474Association analysis for quantitative traits by data mining: QHPM.Ann Hum Genet2002
11793743Mining associations between genetic markers, phenotypes, and covariates.Genet Epidemiol2001
11793763Bayesian association mapping for quantitative traits in a mixture of two populations.Genet Epidemiol2001
10878475Estimation of transmission probabilities in families ascertained through a proband with variable age-at-onset disease: application to the HLA A, B and DR loci in Finnish families with type 1 diabetes. The DiMe Study Group.Hum Hered2000
10848493Data mining applied to linkage disequilibrium mapping.Am J Hum Genet2000
10597524A Bayesian Markov chain Monte Carlo approach to map disease genes in simulated GAW11 data.Genet Epidemiol1999
10587856Neonatal anthropometric measurements and risk of childhood-onset type 1 diabetes. DiMe Study Group.Diabetes Care1999
10651256Worldwide increase in incidence of Type I diabetes--the analysis of the data on published incidence trends.Diabetologia1999
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Collaborators

University of Helsinki
Co-authored papers 13
Folkhalsan Research Center, University of Helsinki
Co-authored papers 13
University of Helsinki
Co-authored papers 7
University of Helsinki
Co-authored papers 6
DocMus Department, University of the Arts Helsinki
Co-authored papers 4
Jarvenpaa Music Institute
Co-authored papers 4
Department of Public Health Solutions, National Institute for Health and Welfare
Co-authored papers 4
Co-authored papers 4
Institute of Human Genetics, University Hospital Bonn
Co-authored papers 2
Philipps University of Marburg
Co-authored papers 2
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Research Institute at Nationwide Childrens Hospital, University of Iowa
Co-authored papers 1
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The Ohio State University
Co-authored papers 1
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Co-authored papers 1
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University of Oslo
Co-authored papers 1
Institute of Human Genetics, University of Bonn and University Hospital Bonn
Co-authored papers 1
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University of Sassari
Co-authored papers 1
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